| Primary Identifier | MGI:1856622 | Allele Type | Spontaneous |
| Gene | Paf | Inheritance Mode | Semidominant |
| Strain of Origin | C3H/HeSn-bc<3J> | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This mutation comprises an inversion of an X chromosome segment with breakpoints distal to Amel and proximal to the PAR marker DXYHgu1. The mutation in this allele is within a ~0.2 cM interval that includes the boundary of the pseudoautosomal region (PAR), a sequence common to the X and Y chromosomes. As a consequence X-Y nondisjunction occurs in hemizygous males, resulting in XO and XXY progeny. |
